Fundamental differences in cell cycle deregulation in human papillomavirus-positive and human papillomavirus-negative head/neck and cervical cancers

被引:378
作者
Pyeon, Dohun
Newton, Nlichael A.
Lambert, Paul F.
den Boon, Johan A.
Sengupta, Srikumar
Marsit, Carmen J.
Woodworth, Craig D.
Connor, Joseph P.
Haugen, Thomas H.
Smith, Elaine M.
Kelsey, Karl T.
Turek, Lubomir P.
Ahlquist, Paul
机构
[1] Univ Wisconsin, McArdle Lab Canc Res, Madison, WI 53706 USA
[2] Univ Wisconsin, Inst Mol Virol, Madison, WI 53706 USA
[3] Univ Wisconsin, Dept Stat, Madison, WI 53706 USA
[4] Univ Wisconsin, Dept Biostat & Med Informat, Madison, WI 53706 USA
[5] Univ Wisconsin, Dept Obstet & Gynecol, Madison, WI 53706 USA
[6] Univ Wisconsin, Howard Hughes Med Inst, Madison, WI 53706 USA
[7] Harvard Univ, Sch Publ Hlth, Dept Genet, Boston, MA 02115 USA
[8] Harvard Univ, Sch Publ Hlth, Dept Complex Dis, Boston, MA 02115 USA
[9] Clarkson Univ, Dept Biol, Potsdam, NY 13699 USA
[10] Vet Affairs Med Ctr, Dept Pathol, Iowa City, IA 52242 USA
[11] Univ Iowa, Dept Epidemiol, Iowa City, IA USA
关键词
D O I
10.1158/0008-5472.CAN-06-3619
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Human papillomaviruses (RPV) are associated with nearly all cervical cancers, 20% to 30% of head and neck cancers (HNC), and other cancers. Because HNCs also arise in HPV-negative patients, this type of cancer provides unique opportunities to define similarities and differences of HPV-positive versus HPV-negative cancers arising in the same tissue. Here, we describe genome-wide expression profiling of 84 HNCs, cervical cancers, and site-matched normal epithelial samples in which we used laser capture microdissection to enrich samples for tumor-derived versus normal epithelial cells. This analysis revealed that HPV+ HNCs and cervical cancers differed in their patterns of gene expression yet shared many changes compared with HPV- HNCs. Some of these shared changes were predicted, but many others were not. Notably, HPV+ HNCs and cervical cancers were found to be up-regulated in their expression of a distinct and larger subset of cell cycle genes than that observed in HPV- HNC. Moreover, HPV+ cancers overexpressed testis-specific genes that are normally expressed only in meiotic cells. Many, although not all, of the hallmark differences between HPV+ HNC and HPV- HNC were a direct consequence of HPV and in particular the viral E6 and E7 oncogenes. This included a novel association of HPV oncogenes with testis-specific gene expression. These findings in primary human tumors provide novel biomarkers for early detection of HPV+ and HPV- cancers, and emphasize the potential value of targeting E6 and E7 function, alone or combined with radiation and/or traditional chemotherapy, in the treatment of HPV+ cancers.
引用
收藏
页码:4605 / 4619
页数:15
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